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Stockholm Myocardial Infarction with Nonobstructive Coronaries Study 3

Not Applicable
Recruiting
Conditions
Myocardial Infarction with Nonobstructive Coronary Arteries
Interventions
Diagnostic Test: Cardiac magnetic resonance imaging to study coronary microvascular dysfunction
Registration Number
NCT05426408
Lead Sponsor
Karolinska Institutet
Brief Summary

The present pilot study will investigate the prevalence of CMD in an unselected cohort of patients with the working diagnosis MINOCA and to study if the diagnostic yield can be improved by adding adenosine to the CMR investigation. Patient will be their own controls.

Detailed Description

Not available

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
85
Inclusion Criteria
  • a suspected diagnosis of MINOCA or takotsubo syndrome with coronary angiography without diameter stenosis β‰₯50%
  • age 35-80 years
  • reading and writing proficiency in Swedish
Exclusion Criteria
  • Claustrofobia
  • Arrythmia and/or pacemaker (atrial fibrillation and AV-block I- III)
  • Asthma or severe chronic obstructive lung disease
  • eGFR < 30 ml/min
  • spontaneous coronary artery dissection
  • acute pulmonary embolism
  • acute myocardial infarction type 2
  • cardiomyopathy other than takotsubo syndrome
  • a previous myocardial infarction due to CAD

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
Patients with MINOCA undergoing CMRCardiac magnetic resonance imaging to study coronary microvascular dysfunctionPatients will be their own controls
Primary Outcome Measures
NameTimeMethod
Diagnostic yieldThrough investigation completion, usually 2 hours

To increase the diagnostic yield of CMR imaging in MINOCA as a working diagnosis

Secondary Outcome Measures
NameTimeMethod
Prevalence of CMD in different final MINOCA diagnosesThrough investigation completion, usually 2 hours

To study the proportions of CMD in patients with a CMR imaging diagnosis of myocardial infarction, Takotsubo, respectively myocarditis and compare them with the results from a healthy control group

Prevalence of CMD in MINOCAThrough investigation completion, usually 2 hours

To determine the proportion of patients with the working diagnosis of MINOCA who have CMD.

Angina pectoris3 Months

To investigate the occurrence of angina pectoris before inclusion and after 3 months and relate it to CMD

Trial Locations

Locations (1)

Per Tornvall

πŸ‡ΈπŸ‡ͺ

Stockholm, Sweden

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